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Cavity exciton-polaritons exhibit ballistic transport and can achieve 100 μm in one picosecond. This ballistic transport significantly enhances mobility compared to that of bare excitons, which often move diffusively and become the bottleneck for energy conversion and transfer devices. Despite being robustly reproduced in experiments and simulations, there is no microscopic theory available for describing the group velocity v of polariton transport and its renormalization. In this work, we derive an analytic expression for v renormalization. The theory suggests the v renormalization is caused by phonon-mediated transitions between the lower polariton (LP) states and the dark states. The theory predicts that the renormalization magnitude depends on both exciton-phonon coupling strength and temperature, which are in quantitative agreement with numerical quantum dynamics simulations. Our results provide theoretical insights and a predictive analytical theory for understanding cavity-enhanced exciton-polariton transport.
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http://dx.doi.org/10.1038/s41467-025-62276-x | DOI Listing |
J Colloid Interface Sci
September 2025
Ministry-of-Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei Key Laboratory of Polymer Materials, School of Materials Science & Engineering, Hubei University, Wuhan 430062, PR China. Electronic address:
Effective removal of ethylene (CH) during fruit and vegetables storage and transport remains a critical challenge for post-harvest preservation. Although S-scheme heterojunctions can improve charge separation and redox capacity for ethylene degradation, their efficiency is still restricted by limited carrier transfer and sluggish oxygen activation. Here, we rationally designed a novel 2D/2D SnNbO/BiMoO monolayer S-scheme heterojunction integrated with Pt co-catalyst to address these limitations.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
September 2025
McKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX 78712.
Many soft, tough materials have emerged in recent years, paving the way for advances in wearable electronics, soft robotics, and flexible displays. However, understanding the interfacial fracture behavior of these materials remains a significant challenge, owing to the difficulty of quantifying the respective contributions from viscoelasticity and damage to energy dissipation ahead of cracks. This work aims to address this challenge by labeling a series of polymer networks with fluorogenic mechanophores, subjecting them to T-peel tests at various rates and temperatures, and quantifying their force-induced damage using a confocal microscope.
View Article and Find Full Text PDFNat Commun
September 2025
Physikalisches Institut, Karlsruhe Institute of Technology, Karlsruhe, Germany.
Precise control of spin states and spin-spin interactions in atomic-scale magnetic structures is crucial for spin-based quantum technologies. A promising architecture is molecular spin systems, which offer chemical tunability and scalability for larger structures. An essential component, in addition to the qubits themselves, is switchable qubit-qubit interactions that can be individually addressed.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Key Laboratory of Eco-chemical Engineering, Ministry of Education, International Science and Technology Cooperation Base of Eco-chemical Engineering and Green Manufacturing, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao, 266042, P. R. China.
Facing the massive energy consumption of over 200 TWh y of chlor-alkali industry, developing high-activity and durable non-precious CER (chlorine evolution reaction) catalysts is urgently needed to address the high overpotentials and suppress the dissolution high-valance metal species. Herein, a carbon quantum dots functionalized trimetallic Fe/Co/Ni spinel oxide nanotube architecture (FCNO@CQDs) is constructed, featuring t-to-π* π-backbonding for dramatically enhanced CER activity and stability. The reverse electron flow from Co d-obritals to the vacant CQDs' π* orbitals can upshift the d-band center for enhanced intermediate adsorption, while stabilizing high-valent Co centers via increased bond order.
View Article and Find Full Text PDFNat Commun
September 2025
Max-Born-Institut für Nichtlineare Optik und Kurzzeitspektroskopie, Berlin, Germany.
Light-induced magnetisation switching is one of the most intriguing and promising areas where an ultrafast phenomenon can be utilised in technological applications. So far, experiment and theory have considered the origin of all-optical helicity-independent magnetisation switching (AO-HIS) in individual magnetic films only as a microscopically local, thermally-driven process of angular momentum transfer between different subsystems. Here, we demonstrate that this local picture is insufficient and that AO-HIS must also be regarded as a spatially inhomogeneous process along the depth within a few-nanometre thin magnetic layer.
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